BEUDAMED
    FDA Enforcement Class II Ongoing

    Juno DRF; Model: 709020 Multi-function x-ray systems capable of routine radiograph and general fluoroscopy procedures.

    Recall: Z-1063-2017 · Reported February 1, 2017

    Enforcement

    Recall Number
    Z-1063-2017
    Event ID
    73459
    Classification
    Class II
    Status
    Ongoing
    Product Type
    Devices
    Firm
    Villa Radiology Systems LLC
    Voluntary / Mandated
    Voluntary: Firm initiated
    Initial Notification
    Letter
    Report Date
    February 1, 2017
    Initiation Date
    February 19, 2016
    Classification Date
    January 20, 2017
    Address
    91 Willenbrock Rd Ste B1, N/A, Oxford, CT, 06478-1036, United States

    Description

    Juno DRF; Model: 709020 Multi-function x-ray systems capable of routine radiograph and general fluoroscopy procedures.

    Reason

    The analysis showed that the incident was caused by a chain of four faults: 1.) The injured person overcame a physical barrier (the tabletop support arm. height ca. 60 em) to access a prohibited area not intended as a working position. 2) The directions for use (device labeling and instructions for use) did not contain an explicit exclusion of the prohibited area. 3.) The movement was activated inadvertently and continuously. and it was not released (the movement requires continuous activation). 4.) Delayed activation of the emergency stop.

    Code Info

    10110770 11030805 11030806 11070845 11070848 11070849 11090864 11110900 12020978 12020982 12030999 12041003 12061014 12061018 12061020 12081040 12091074 12101104 12121186 12121187 13031215 13101263 14021301 14031313 14041321 14051332 14071353 14081359 14091368 14091371 14121400 14121403 15021426 15031440 15041444 15091473 15091478 15101484 15101487

    Distribution

    AL AZ CA CO CT DC FL IA IL IN LA MA MD MI MN MO MS NJ NY OH PA Puerto Rico TN TX UT WI

    Quantity

    66 distributed in US